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Volumn , Issue 3, 1999, Pages 607-616

The reduction of α-X-acetophenones (X = PhO, Br, Cl) in hydrogendonating solvents at elevated temperatures

Author keywords

Bond dissociation enthalpies; DFT; Hydrogen donor; Lignin; Phenacyl halides

Indexed keywords

ACETOPHENONE DERIVATIVE; ALPHA PHENOXYACETOPHENONE; PHENACYL BROMIDE; UNCLASSIFIED DRUG;

EID: 0032771275     PISSN: 1434193X     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (15)

References (81)
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    • p value (by calculating the frequencies also at 1100 K) because the calculation time was much shorter than that for BrAP.
    • p value (by calculating the frequencies also at 1100 K) because the calculation time was much shorter than that for BrAP.
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    • Addition of ketyl radicals in 2-propanol to the olefinic moiety in the enol may explain the formation of the side products and is in accordance with the structural elements as detected by GCMS analysis.
    • Addition of ketyl radicals in 2-propanol to the olefinic moiety in the enol may explain the formation of the side products and is in accordance with the structural elements as detected by GCMS analysis.
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    • [46] or eliminate a proton yielding styrene. Polymerization of styrene is very fast at the applied temperatures and may render a low mass balance.
    • [46] or eliminate a proton yielding styrene. Polymerization of styrene is very fast at the applied temperatures and may render a low mass balance.
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    • note
    • -1, which has been derived from the addition of phenoxyl to styrene, may well be higher for aliphatic systems.
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    • unpublished results
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    • -1.
    • -1.
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    • [33], p. 90.
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    • -1.
    • -1.
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    • -8 M (see text).
    • -8 M (see text).
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    • -1.
    • -1.
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.